(E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide

The title compound, C(8)H(9)ClN(4)S, which has potential insecticidal activity, was synthesized by the reaction of 2-chloro-5-methyl­nicotinaldehyde and thio­semicarbazide. In the crystal structure, the mol­ecules are linked via inter­molecular N—H⋯N, N—H⋯S and N—H⋯Cl hydrogen bonds, forming a three...

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Detalles Bibliográficos
Autores principales: Wang, Zhen, Ma, Yongqiang, Xu, Yan, Ling, Yun, Yang, Xinling
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983548/
https://www.ncbi.nlm.nih.gov/pubmed/21580363
http://dx.doi.org/10.1107/S1600536810004915
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author Wang, Zhen
Ma, Yongqiang
Xu, Yan
Ling, Yun
Yang, Xinling
author_facet Wang, Zhen
Ma, Yongqiang
Xu, Yan
Ling, Yun
Yang, Xinling
author_sort Wang, Zhen
collection PubMed
description The title compound, C(8)H(9)ClN(4)S, which has potential insecticidal activity, was synthesized by the reaction of 2-chloro-5-methyl­nicotinaldehyde and thio­semicarbazide. In the crystal structure, the mol­ecules are linked via inter­molecular N—H⋯N, N—H⋯S and N—H⋯Cl hydrogen bonds, forming a three-dimensional network stacked down a.
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spelling pubmed-29835482010-12-30 (E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide Wang, Zhen Ma, Yongqiang Xu, Yan Ling, Yun Yang, Xinling Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(8)H(9)ClN(4)S, which has potential insecticidal activity, was synthesized by the reaction of 2-chloro-5-methyl­nicotinaldehyde and thio­semicarbazide. In the crystal structure, the mol­ecules are linked via inter­molecular N—H⋯N, N—H⋯S and N—H⋯Cl hydrogen bonds, forming a three-dimensional network stacked down a. International Union of Crystallography 2010-02-13 /pmc/articles/PMC2983548/ /pubmed/21580363 http://dx.doi.org/10.1107/S1600536810004915 Text en © Wang et al. 2010 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Wang, Zhen
Ma, Yongqiang
Xu, Yan
Ling, Yun
Yang, Xinling
(E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide
title (E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide
title_full (E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide
title_fullStr (E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide
title_full_unstemmed (E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide
title_short (E)-1-[(2-Chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide
title_sort (e)-1-[(2-chloro-5-methyl­pyridin-3-yl)methyl­ene]thiosemicarbazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983548/
https://www.ncbi.nlm.nih.gov/pubmed/21580363
http://dx.doi.org/10.1107/S1600536810004915
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